MEDLINE INDUSTRIES, LP - Northfield 2024-02-07 Health serious FDA
Health · FDA · Recall #FDA-Z-0967-2024
MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723 Recall
Issued February 7, 2024 · MEDLINE INDUSTRIES, LP - Northfield
In February 2024, MEDLINE INDUSTRIES, LP - Northfield recalled the MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
What you should do
- 1 Stop using MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact MEDLINE INDUSTRIES, LP - Northfield to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Category
- Health
- Recall date
- February 7, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-0967-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- MEDLINE INDUSTRIES, LP - Northfield has 108 recalls in our database, including 12 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.